Search results for "steric"

showing 10 items of 476 documents

The reaction of optically active α-aminocarboxylic acid hydrazides with triethyl orthoesters

2011

New derivatives of 2-(1-amino-1-phenylmethyl)-1,3,4-oxadiazole and 1,2,4-triazin-6-one were synthesised in the reactions of optically active α-aminocarboxylic acid hydrazides and triethyl orthoesters in xylene. The electronic and steric effects of substituents at the α position influencing the formation of five- or six-membered products are discussed.

Steric effectschemistry.chemical_compoundchemistryOrganic ChemistryDrug DiscoveryXyleneOptically activeBiochemistryMedicinal chemistryTetrahedron
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3-(Pyridin-2-yl)[1,2,3]triazolo[1,5-a]quinoline: A Theoretical and Experimental Analysis of Ring-Chain Isomerisation

2009

In the course of the synthesis of new fluorophores for molecular recognition an experimental (1H NMR) and theoretical (DFT) study of the ring-chain isomerism of 3-(pyridin-2-yl)[1,2,3]triazolo[1,5-a]quinoline derivatives (A) into 2-([1,2,3]triazolo[1,5-a]pyridin-3-yl)quinoline derivatives (B) has been carried out. The rearrangement is influenced by steric and electronic effects of the substituents present on the quinoline ring. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)

Steric effectschemistry.chemical_compoundchemistryStereochemistryMetalationOrganic ChemistryQuinolineProton NMRElectronic effectPhysical and Theoretical ChemistryRing (chemistry)Chemical synthesisIsomerizationEuropean Journal of Organic Chemistry
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Tunable Spin-Crossover Behavior of the Hofmann-like Network {Fe(bpac)[Pt(CN) 4 ]} through Host-Guest Chemistry

2013

A study of the spin-crossover (SCO) behavior of the tridimensional porous coordination polymer {Fe(bpac)[Pt(CN)4]} (bpac=bis(4-pyridyl) acetylene) on adsorption of different mono- and polyhalobenzene guest molecules is presented. The resolution of the crystal structure of {Fe(bpac)[Pt(CN) 4]}A?G (G=1,2,4-trichlorobenzene) shows preferential guest sites establishing I?A?A?A?I? stacking interactions with the host framework. These host-guest interactions may explain the relationship between the modification of the SCO behavior and both the chemical nature of the guest molecule (electronic factors) and the number of adsorbed molecules (steric factors). Copyright © 2013 WILEY-VCH Verlag GmbH & …

Steric effectsclathrates010405 organic chemistryCoordination polymerStereochemistryOrganic Chemistryhost–guest systemsStackingGeneral ChemistryCrystal structure010402 general chemistrystacking interactions01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundCrystallographymetal–organic frameworkschemistryspin crossoverSpin crossoverMoleculeMetal-organic framework[CHIM.COOR]Chemical Sciences/Coordination chemistryHost–guest chemistry
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Shedding Light on the Interactions of Hydrocarbon Ester Substituents upon Formation of Dimeric Titanium(IV) Triscatecholates in DMSO Solution

2020

Abstract The dissociation of hierarchically formed dimeric triple lithium bridged triscatecholate titanium(IV) helicates with hydrocarbyl esters as side groups is systematically investigated in DMSO. Primary alkyl, alkenyl, alkynyl as well as benzyl esters are studied in order to minimize steric effects close to the helicate core. The 1H NMR dimerization constants for the monomer–dimer equilibrium show some solvent dependent influence of the side chains on the dimer stability. In the dimer, the ability of the hydrocarbyl ester groups to aggregate minimizes their contacts with the solvent molecules. Due to this, most solvophobic alkyl groups show the highest dimerization tendency followed by…

Steric effectscoordination compoundsesteritDimersolvent effects010402 general chemistry01 natural sciencesMedicinal chemistryCatalysishelicatechemistry.chemical_compoundthermodynamicshelicate thermodynamicsSide chainMoleculeAlkylchemistry.chemical_classificationCoordination Chemistry | Hot PaperFull Paper010405 organic chemistryOrganic ChemistrykompleksiyhdisteetGeneral ChemistryFull PapersTriple bond0104 chemical sciences3. Good healthchemistrytermodynamiikkaweak interactionsSolvent effectsSolvophobicChemistry (Weinheim an Der Bergstrasse, Germany)
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Crystal structure of 4-[(adamantan-1-yl)amino]­naphthalene-1,2-dione

2019

The title compound, an example of a stable 1,2-naphtho­quinone, illustrates steric buttressing of the adamantanyl group.

Steric effectscrystal structureAdamantaneintra­molecular hydrogen bondingadamantanenaphthoquinoneAdamantaneCrystal structureN— HO hydrogen bonding010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciencesResearch CommunicationsCrystallcsh:ChemistryDelocalized electronchemistry.chemical_compoundNaphthoquinoneGroup (periodic table)General Materials ScienceNaphthaleneintramolecular hydrogen bondingCrystal structurenaphtho­quinone548.81 Cristalografía estructuralIntramolecular hydrogen bondingGeneral ChemistryCondensed Matter PhysicsNaphthoquinone0104 chemical sciencesCrystallographychemistrylcsh:QD1-999N—H...O hydrogen bondingN—H⋯O hydrogen bondingActa Crystallographica Section E: Crystallographic Communications
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Substituent effects in trans-p,p'-disubstituted azobenzenes: X-ray structures at 100 K and DFT-calculated structures.

2014

The crystal and molecular structures of twopara-substituted azobenzenes with π-electron-donating –NEt2and π-electron-withdrawing –COOEt groups are reported, along with the effects of the substituents on the aromaticity of the benzene ring. The deformation of the aromatic ring around the –NEt2group inN,N,N′,N′-tetraethyl-4,4′-(diazenediyl)dianiline, C20H28N4, (I), may be caused by steric hindrance and the π-electron-donating effects of the amine group. In this structure, one of the amine N atoms demonstrates clearsp2-hybridization and the other is slightly shifted from the plane of the surrounding atoms. The molecule of the second azobenzene, diethyl 4,4′-(diazenediyl)dibenzoate, C18H18N2O4,…

Steric effectscrystal structureChemistryStereochemistry4electron-donating effectsSubstituentAromaticityCrystal structureDFT calculationsCondensed Matter PhysicsInorganic ChemistryCrystalelectron-withdrawing effectsHOMA indexCrystallographychemistry.chemical_compoundMaterials Chemistry4'-(diazenediyl)dibenzoateAmine gas treatingDensity functional theoryPhysical and Theoretical Chemistryazo­benzenesBenzene4'-(diazene­diyl)dianilineActa crystallographica. Section C, Structural chemistry
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Crystal structure of N-(tert-butoxycarbonyl)phenylalanyldehydroalanine isopropyl ester (Boc–Phe–ΔAla–OiPr)

2014

In the crystal structure of the de­hydro­dipeptide (Boc-Phe-ΔAla-OiPr), the mol­ecule has a trans configuration of the N-methyl­amide group. Its geometry is different from saturated peptides but is in excellent agreement with other de­hydro­alanine compounds. In the crystal, an N—H⋯O hydrogen bond links the mol­ecules in a herringbone packing arrangement.

Steric effectsde­hydro­alaninecrystal structurede­hydro peptidesCrystal structureResearch Communicationslcsh:Chemistrychemistry.chemical_compoundDehydroalanineαβ-dehydroamino acidsPeptide bondMoietyGeneral Materials ScienceHydrogen bond[alpha]General Chemistrydehydroalaninedehydro peptidesCondensed Matter Physicsherringbone packing[beta]-de­hydro­amino acidsCrystallographyMolecular geometrychemistrylcsh:QD1-999αβ-de­hydro­amino acidsIsopropylActa Crystallographica Section E
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Planar-Chiral 1,1 '-Diboryl Metallocenes: Diastereoselective Synthesis from Boryl Cyclopentadienides and Spin Density Analysis of a Diborylcobaltocene

2017

International audience; The reaction of nonsubstituted alkali metal cyclopentadienides with haloboranes leads to similar to 90:10 mixtures of isomeric diene products that can be deprotonated to give simple boryl cyclopentadienides. We extended this transformation to the sterically hindered lithium tert-butylcyclopentadienide 1 using FBMe(s)2 (Mes = 2,4,6-trimethylphenyl) and ClBCy2 as electrophiles. The boryl group is selectively introduced in the remote position to minimize steric congestion. The new boryl dienes are obtained as mixtures of isomers, and subsequent deprotonation with MeLi or LiHMDS affords the lithium 1,3-disubstituted cyclopentadienides Sa,b in yields over 95%. Direct asse…

Steric effectselectronDienechemistry.chemical_elementanion recognition[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistryPhotochemistryligand01 natural sciencesMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundDeprotonationredox chemistryCobaltocenePhysical and Theoretical ChemistryConformational isomerismbidentate lewis-acids010405 organic chemistryChemistryDiastereomercrystal-structure[ CHIM.INOR ] Chemical Sciences/Inorganic chemistry0104 chemical sciencessubstituted ferrocenesElectrophileLithiumactivationolefin polymerizationboron
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Azide Binding Controlled by Steric Interactions in Second Sphere. Synthesis, Crystal Structure, and Magnetic Properties of [Ni II 2 (L)(μ 1,1 -N 3 )]…

2016

International audience; The dinuclear Ni-II complex [Ni-2(L-2)][ClO4](2) (3) supported by the 28-membered hexaaza-dithiophenolate macro-cycle (L-2)(2-) binds the N-3(-) ion specifically end-on yielding [Ni-2(L-2)(mu(1,1)-N-3)] [ClO4] (7) or [Ni-2(L-2)(mu(1,1)-N-3)][BPh4] (8), while the previously reported complex [Ni2L1(mu(1,3)-N-3)][ClO4] (2) of the 24-membered macrocycle (L-1)(2-) coordinates it in the end-to-end fashion. A comparison of the X-ray structures of 2, 3, and 7 reveals the form-selective binding of complex 3 to be a consequence of its preorganized, channel-like binding pocket, which accommodates the azide anion via repulsive CH center dot center dot center dot pi interactions …

Steric effectsequilibrium-constantsStereochemistrytransition-metal-complexesCrystal structure010402 general chemistry01 natural sciences[ CHIM ] Chemical Sciencessolvation free-energyInorganic Chemistrychemistry.chemical_compoundtetranuclear nickel(ii) complexes[CHIM.CRIS]Chemical Sciences/CristallographyAntiferromagnetismMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical Chemistrymu-azidoEquilibrium constantmolecular-structure010405 organic chemistryChemistryLigandni-ii[ CHIM.INOR ] Chemical Sciences/Inorganic chemistryend-to-end0104 chemical sciencesexchange interactionsCrystallographyAzideGround stateorbital interactions[ CHIM.RADIO ] Chemical Sciences/Radiochemistry
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Performances of symmetrical achiral ferrocenylphosphine ligands in palladium-catalyzed cross-coupling reactions: A review of syntheses, catalytic app…

2007

Abstract Ferrocene derivatives bearing donor atoms led to the generation of several classes of metallo-ligands, which collectively show an impressive diversity of applications, especially in metal-catalyzed modern organic reactions. Based on the impetus provided by the use of the diphosphine 1,1′-bis(diphenylphosphino)ferrocene (dppf) the investigations directed towards the synthesis of new ferrocenylphosphines remain of fundamental and industrial interest. The present review aims to describe the performances in palladium-catalyzed cross-coupling reactions of symmetrical achiral ferrocenylphosphine ligands, mainly diphosphines. We specifically choose to restrict our review efforts to these …

Steric effectsferrocenylphosphine -palladiumSonogashira couplingBite angle010402 general chemistry01 natural sciencesCoupling reactionInorganic Chemistry[ CHIM.CATA ] Chemical Sciences/Catalysischemistry.chemical_compoundcross-coupling reactionsDiphosphinesMaterials ChemistryOrganic chemistrystructurePhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUScatalysis010405 organic chemistryNegishi coupling[CHIM.CATA]Chemical Sciences/CatalysisCombinatorial chemistry0104 chemical sciencesreactivityOrganic reactionFerrocenechemistryCoordination Chemistry Reviews
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